Novel Thiazolyl Azo Dyes: Elucidating the Design, Synthesis, Spectral Characterization, Cytotoxicity, and Antibacterial Potential of its Co(III), Ni(II), and Cu(II) NanoComplexes

被引:2
作者
Majhool, Suha Hassan [1 ]
Waheeb, Azal Shakir [1 ]
Ali Awad, Masar [1 ]
机构
[1] Univ Al Muthanna, Coll Sci, Dept Chem, Samawah, Iraq
关键词
Cell line; Characterization; Metals; Nanocomplxes; TRANSITION-METAL-COMPLEXES; DERIVATIVES; MN(II); DONOR;
D O I
10.22052/JNS.2024.02.004
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
2-[2-(5-Methylethiazolyl) azo] and the combination of its cobalt(III), nickel(II), and copper(II) complexes yields the new bidentate azo dye ligand 5,6-dimethylbenzimidazole (5-MeTADMBI). The suggested structures were found by using atomic absorption spectroscopy, molar conductivity, magnetic susceptibility, nuclear magnetic resonance (1H NMR) and 13C NMR, Fourier transforms infrared (FTIR), ultraviolet-visible (UV-Vis), mass spectrometry, X-ray diffraction (XRD), thermogravimetric analysis (TGA/DTG), and scanning electron microscope field emission (FESEM). All complexes have been given geometry suggestions according to analytical and spectroscopic data with cobalt(III), nickel(II), and copper(II) ions, the 5-MeTADMBI ligand takes an octahedral shape via N, N donors and behaves as a bidentate. The biological testing of the synthesized compounds against Escherichia coli, Staphylococcus aureus, Klebsiella and candida. revealed increased antibacterial activity. Their testing revealed that the metal complexes are superior against a variety of bacterial and fungal species. Finally, based on IC50, most of the compounds exhibited potent anticancer activity towards both the A549 human lung cancer cell line and the normal human lung fibroblast HdFn cell line.
引用
收藏
页码:392 / 410
页数:19
相关论文
共 55 条
[21]  
Basim Sura, 2023, Asian Pac J Cancer Prev, V24, P581, DOI 10.31557/APJCP.2023.24.2.581
[22]   Classifications, properties, recent synthesis and applications of azo dyes [J].
Benkhaya, Said ;
M'rabet, Souad ;
El Harfi, Ahmed .
HELIYON, 2020, 6 (01)
[23]   Synthesis, structure elucidation and dft study of a new thiazole-pyridine anchored nnn donor and it's cobalt(II) complex: In-vitro antitumor activity against U937 cancer cells, dna binding property and molecular docking study [J].
Bera, Pradip ;
Aher, Abhishek ;
Brandao, Paula ;
Manna, Sunil Kumar ;
Bhattacharyya, Indranil ;
Pramanik, Chandana ;
Mandal, Basudev ;
Das, Satyabrata ;
Bera, Pulakesh .
JOURNAL OF MOLECULAR STRUCTURE, 2021, 1224
[24]   Comparison in optoelectronic properties of triphenylamine-imidazole or imidazole as donor for dye-sensitized solar cell: theoretical approach [J].
Bourouina, Assia ;
Rekis, Maammar .
JOURNAL OF MOLECULAR MODELING, 2021, 27 (08)
[25]   Origin of the Bathochromic Shift of Astaxanthin in Lobster Protein: 2D Electronic Spectroscopy Investigation of β-Crustacyanin [J].
Christensson, Niklas ;
Zidek, Karel ;
Magdaong, Nikki Cecil M. ;
LaFountain, Amy M. ;
Frank, Harry A. ;
Zigmantas, Donatas .
JOURNAL OF PHYSICAL CHEMISTRY B, 2013, 117 (38) :11209-11219
[26]   Design, synthesis, and biological evaluation of a novel series of thiazole derivatives based on pyrazoline as anticancer agents [J].
Fathy, Usama ;
Yousif, Mahmoud N. M. ;
El-Deen, Eman M. Mohi ;
Fayed, Eman A. .
EGYPTIAN JOURNAL OF CHEMISTRY, 2022, 65 (13) :1241-1252
[27]   Novel indole-thiazole and indole-thiazolidinone derivatives as DNA groove binders [J].
Ferreira Alves, Josival Emanuel ;
de Oliveira, Jamerson Ferreira ;
Couto de Lima Souza, Tulio Ricardo ;
de Moura, Ricardo Olimpio ;
de Carvalho Junior, Luiz Bezerra ;
Alves de Lima, Maria do Carmo ;
Vitalino de Almeida, Sinara Monica .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2021, 170 :622-635
[28]   New strategy for the preparation of imidazole derivatives containing thiazole ring via ring opening/coupling/cyclization/decarboxylation cascade [J].
Golestaneh, Zahrasadat ;
Ghashang, Majid .
TETRAHEDRON LETTERS, 2019, 60 (44)
[29]  
Hameed G, 2020, Egyptian Journal of Chemistry
[30]   Synthesis, characterization and electrochemical studies of azo dyes derived from barbituric acid [J].
Harisha, S. ;
Keshavayya, Jathi ;
Swamy, B. E. Kumara ;
Viswanath, C. C. .
DYES AND PIGMENTS, 2017, 136 :742-753